SECTION IV VOLUNTARY CERTIFICATION SCHEME FOR AYUSH PRODUCTS Certification Process

1. SCOPE OF THIS DOCUMENT This document explains the process of certification under the Voluntary Certification Scheme for Ayush Products (hereinafter referred to as the Scheme) and the requirements that should be followed in order to obtain, operate and maintain the Certification. OBJECTIVE The objective of this document is to regulate the operation of the Scheme and promote uniformity in its operation and the interaction between the Certification Bodies (from now on CBs), the manufacturing organizations seeking product certification and the Department of Ayush. SCOPE OF CERTIFICATION The Ayush Certification is awarded at two levels: a) Ayush Standard Mark which is based on compliance to the domestic regulatory requirements; and b) Ayush Premium Mark which is based on either or both of the following options; Option A: Compliance to the GMP Requirements based on WHO Guidelines and Levels of contaminants as given in Certification Criteria document. Note i.

2.

3. 3.1

ii.

The requirements of heavy metals shall not be applicable to Ayush products having raw materials of metallic origin provided they are intended for domestic market. For the time being this certification is available for Herbal products only.

Option B: Compliance to regulatory requirements of any importing country provided these are more stringent than Option A above. Note i.

For the time being this certification is available for Herbal products

3.1.1 For any manufacturer to qualify for Ayush Premium Mark certification, compliance to the domestic regulation and having inhouse testing facilities is a prerequisite. 3.2 The elements of the Certification process are: a) evaluation of the manufacturing facility for manufacturing and hygiene processes, and capability to manufacture Ayush products of a desired quality on a continuous basis, SectionIVCertificationProcessVersion1 Page1of13

b) evaluation of the quality of the Ayush product(s) for compliance to relevant certification criteria through testing of products sampled from the manufacturing facility and the market or any other source. 3.3 The Scheme is open to all manufacturing organizations that are legal entities in India. 3.4 The Department of Ayush itself is not involved in the certification of Ayush products. It is the owner of the Certification Scheme, Certification Criteria and the Certification Mark(s). Certification is operated by independent product certification bodies duly accredited by NABCB and/or recommended by QCI. 3.5 The process by which a manufacturing organization gains and maintains certification is summarized in the document Steps for obtaining Certification for Ayush Products. The entire process of how to obtain certification of Ayush products is also available on the website of Department of Ayush (www.) as well as QCI (www.qcin.org). 3.6 The certification to the above mentioned criteria shall be carried out by the CBs duly accredited for the certification scheme as per ISO/IEC Guide 65, by NABCB and/or recommended by QCI. To operate under the Scheme the CBs will require an extension of scope within the accreditation for ISO/IEC Guide 65 and comply with the provisions of the document Requirements for Certification Bodies. 4. 4.1 4.1.1 CERTIFICATION PROCESS Registration of Application The certification body shall maintain and make publicly available accurate information describing its certification processes for granting, maintaining, extending, renewing, reducing, suspending or withdrawing product certification, and geographical areas in which it operates The information shall include reference to the Certification Criteria, procedure for obtaining Ayush Product Certification, a detailed description of the initial and continuing certification activity, including the application, initial evaluation, periodic surveillance evaluations, and the process for granting, maintaining, reducing, extending, suspending, withdrawing certification and recertification . an Application form; list of documents required to be submitted along with the application. information about the fee for application, initial certification and continuing certification documents describing the rights and duties of certified clients, and information on procedures for handling complaints and appeals The CB shall respond to all enquiries received from prospective applicants for Ayush product certification with complete information for facilitating a registration of an applicant, within seven days of receipt of the query. The prospective applicant organization manufacturing Ayush products shall apply to the Certification Body on the Application format prescribed by the CB, and provide as a minimum information on the name and address of applicant with contact details, proof of legal entity, location of manufacturing unit, products being manufactured, products and dosage form for which certification is being sought, relevant certification criteria against which certification is being sought, description of production processes, own installed/existing manufacturing and testing facilities, number of SectionIVCertificationProcessVersion1 Page2of13

a) b)

c) d) e) f) g) 4.1.2

4.1.3

shifts of operation, number and competence of manpower, and accessibility to external testing facilities, if required. The prospective applicant must confirm that the production facility has been in production for at least one year, and that five commercial batches of the products of dosage form for which certification is being sought, have been manufactured during the current licensed period.The prospective applicant organization shall declare whether it has been an applicant/certified under this Scheme with or by any other certification body, and if yes then shall provide the previous evaluation reports to the new certification body. The certification body may verify the information provided by contacting the earlier certification body. 4.1.4 The prospective applicant organization shall along with the application declare any judicial proceedings relating to its operations/product, any proceedings by any Regulatory body or suspension/cancellation/withdrawal of any certification/approvals under any Regulations or otherwise. 4.1.5 Certification is granted only against the current relevant certification criteria. The certification body shall review all applications for the above and ensure the same. 4.1.6 All applications for certification shall be reviewed by the certification body for adequacy and deficiencies observed, if any, shall be informed to applicant organization within seven days of receipt of application. Review of applications shall be done by a competent person. Records of review shall be maintained. 4.1.7 Only applications found to be completely filled and supported with all documents sought shall be accepted and registered in order of receipt with a unique identification number, acknowledged and records maintained. Registration shall be done within seven days of receipt of application or deficiencies communicated as per 4.1.6 above. 4.1.8 Antecedents of the applicants shall be checked in relation to the Scheme. If the manufacturing licence has been suspended / cancelled for a product or the factory during the last one year, the application from the same organization shall not be entertained. 4.1.9 Applications from organizations who have earlier either misused the Ayush Certification Mark, or have been implicated / convicted by the court, or whose earlier certificate was cancelled because of violation of terms & conditions/misuse of certification mark shall not be registered within three years of conviction/strictures by the court/cancellation of the certificate by any CB. 4.1.10 Applications from organizations found to be misusing the Ayush Certification Mark while their application is being processed for grant if certificate, shall not be processed any further, and rejected after a due notice of 15 days. Fresh applications from them shall be treated as per clause 4.1.9 given above. 4.1.11 Requests for grant of certificates from ex applicants shall be processed like a fresh applicant and the entire procedure for grant of certificate be adhered to subject to clauses 4.1.8, 4.1.9 and 4.1.10 above. 4.1.12 Certification Bodies shall reject or close all Application under the following conditions; a) if Initial Evaluation is not carried out within six months of registration of application b) if more than 20% of samples fail on factory testing during the Initial Evaluation and during the follow up Evaluation carried out after organization has confirmed necessary corrective actions. SectionIVCertificationProcessVersion1 Page3of13

c) If testing facilities are not completed within three months of Initial Evaluation, or else arrangements for testing for specified requirements in NABL accredited laboratories have not been made; d) Non acceptance of internal quality assurance protocol within a month of Initial Evaluation; e) Lack of competent personnel for production and testing, f) If organizations shows no progress towards completion of corrective actions within three months of Initial Evaluation and six months of Registration of application. g) Misuse of Ayush Certification Mark h) Evidence of malpractice i) Voluntary withdrawal of application. 4.1.13 In the event of a closure/rejection of an Application, the application fee submitted with the application may be refunded as decided by the certification body. 4.2 Initial Evaluation 4.2.1 Initial evaluation shall be carried out by a competent evaluation team in one stage for the Ayush Standard Mark and two stages for the Ayush Premium Mark. 4.2.2 The certification body shall communicate the composition of the teams to the applicant organization for identification of conflict of interest if any. Any objections to the team by the applicant should be examined on merit. 4.2.3 Timings and date of Initial Evaluation shall be fixed in consultation with the organization ensuring that production processes representative of normal operations will be open for witnessing during the planned Evaluations. The duration and plan for Initial Evaluation shall be provided to the applicant. 4.2.4 Initial Evaluation of the product and the processes at the site of the applicant shall be conducted within one month of registration of application and or satisfactory fulfilment of all application requirements. 4.2.5 In the initial evaluation for Ayush Standard Mark, the certification body shall list the applicable domestic regulatory requirements, verify compliance to the certification criteria and also verify competence of testing personnel and the testing facility by witnessing testing of sample(s) in the laboratory of the organization, if available. 4.2.6 During the Stage 1 evaluation for Ayush Premium Mark, the certification body shall list the applicable regulatory requirements, check the applicants compliance to these requirements on a sampling basis, status of GMPs, availability of competent personnel and adequate equipment for production and testing, availability of production and test records, the validation records and the state of preparedness for the Stage 2 evaluation, and prepare a report. 4.2.7 Deficiencies observed with respect to the certification criteria during the Stage 1 evaluation shall be informed in writing to the applicant. 4.2.8 The Stage 2 evaluation by certification body shall take place only after necessary actions on the identified deficiencies have been taken and confirmed by applicant. The CB may seek documentary evidence or organize an onsite visit, if necessary, to verify the implementation of corrective actions. 4.2.9 During the Stage 2 evaluation of the applicant, the team shall a) Verify and report compliance to the applicable certification criteria

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b) Witness the production processes covering as many products applied for as possible; c) Check for process controls being exercised for dosage forms and products under certification for ensuring Product quality and conformance to regulatory requirements and undertake verification of all production and test records; d) If satisfied with b) above, draw samples of each dosage form Ayush product offered for certification, ensuring they are representative of normal production capability, as per sampling plan given below for testing in the factory as well for testing in an independent laboratory; e) Check the availability of testing facilities in the manufacturing facility for adequacy; f) Witness the testing of at least one sample(s) drawn for relevant important characteristics possible that can be tested in the factory testing laboratory for compliance to applicable certification criteria; If sample fails on factory testing, fresh sample to be drawn for factory and independent testing only after the organization has initiated a root cause analysis followed by corrective actions; g) Verify competence of testing personnel and the testing facility by witnessing testing of the sample in the laboratory of the organization. h) Draw samples for independent testing, as far as possible not to be from the same Batch as the sample drawn for factory testing; i) Take care that Sample is drawn in such a manner so as not to contaminate the product while sampling and packing. j) Pack and seal the samples(s) such that the product integrity is maintained for its intended shelf life. k) Clearly identify the samples with their name and type, Batch identification and suitable identification to enable traceability to the applicant and the Initial Evaluation visit l) Mask the identity of the sample with respect to its Brand name, and the name of manufacturer as depicted on the original packing. m) Draw samples in quantities adequate to facilitate their testing for all requirements specified in the Criteria. n) Ensure that if the product is affected by the conditions of temperature, handling and storage, the sample is drawn and maintained under those conditions for testing its conformity to specified criteria. 4.2.10 The certification body shall draw at least one sample of the product from one or more dosage forms for factory testing for establishing its capability to test, and sample at least 25% of the products offered within the dosage form for independent testing. 4.2.11 Any non conformities observed during Stage 2 evaluation with respect to the certification criteria shall be informed in writing to the applicant for taking necessary action. The non conformities shall be classified as Major or Minor depending on their severity. 4.2.12 A non conformity is classified as Major when it relates directly to the quality of the product and the manufacturing organizations capability to produce a product that would conform to the certification criteria.

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4.2.13 A non conformity is classified as Minor when it relates to other implementation issues which do not directly affect either the quality of the product or the manufacturing organizations capability to produce a product conforming to the certification criteria. 4.2.14 Sample of each of the Ayush product drawn for independent testing shall be forwarded to an NABL accredited testing laboratory for ascertaining conformance to specified criteria. The specified criteria shall be clearly mentioned and communicated to the testing laboratory. The samples(s) shall be duly coded and as far as possible, the identity of the manufacturer shall be hidden. The sample(s) shall be so despatched that they do not get damaged and or contaminated, undergo deterioration, and the product integrity is maintained. 4.2.15 Certification Body shall maintain records of all certification activities application registration, documents provided by applicant, on site evaluation report including factory testing results, Test reports of sample sent for independent testing. 4.2.16 An internal quality assurance protocol for controlling the quality of the Ayush product(s) during various stages of production up to its despatch based on the general Internal Quality Assurance Protocol given under this scheme shall be developed by the CB for each product/product group and given to the applicant. The applicants consent to comply with the same shall be obtained. This protocol advises the manufacturer on the protocol to be adopted for ensuring the quality of the Ayush products. This protocol covers the following; a) Definition of a Batch ; b) The frequency of tests on the raw material, if necessary , c) The controls at the intermediate stages of manufacture , d) The parameters of quality and contaminants as specified in the applicable certification Criteria, e) Criteria for the conformity of the Batch to the various requirements of the applicable certification Criteria, f) Sample size, g) Frequency of testing, h) Method of testing, i) List of instruments/equipments requiring periodic calibration, j) Compliance to Regulatory requirements, k) Records to be maintained. l) The format for maintaining test and other relevant records and m) Method of applying the Ayush Mark of Conformity on the product including Not for Export on all products intended for domestic market 4.2.17 The internal quality assurance protocol is a dynamic document and shall be reviewed and amended, if required, as when the certification criteria undergo modifications and revisions or otherwise. The date of implementation of the revised internal quality assurance protocol shall be communicated to applicants to the product certification scheme and to the manufacturing unit that have been certified by the CB under this scheme. 4.2.18 A Brand Name declaration shall be obtained from the applicant indicating the Brand names the manufacturer intends to use on products covered under the Ayush Certification Scheme. The applicant shall have to provide proof of ownership of the

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4.3 4.3.1

4.3.2

4.3.3

4.3.4

Brand name, and to facilitate any product recall if such a situation were ever to arise during the operation of the certification of scheme.. Grant of Certificate The certification body shall ensure the following prior to processing the application for grant of certificate : a) The availability of all relevant manufacturing and processing equipment required for the production/manufacture of Ayush products. b) Availability of authorized and/or adequate power and water supplies, where such supplies are required for manufacturing and testing. c) A test laboratory fully equipped to check all quality characteristics and contaminants of the Ayush products strictly in accordance with the prescribed test procedure or an arrangement to have the same tested form an NABL accredited laboratory with the scope covering testing of Ayush products. d) Competent and qualified personnel for production and testing of Ayush product(s). e) Conformity of the product and raw material wherever specified, with parameters/ requirements of the certification criteria; f) Acceptance from the applicant for following the internal quality assurance protocol, for the products for which product certification is being sought; g) Necessary documentation for proof of legal entity and authentication of premises of manufacture where certification is being sought. h) Verification of the applicants production facility having been in production for at least one year. i) Verification of the applicant having manufactured at least five commercial batches of the products of dosage form for which certification is being sought during the current licensed period. j) Acceptance from the applicant for other certification requirements like the fee, Brand name declaration, etc . k) Verification of implementation of corrective actions through a follow up evaluation on site in case of major non conformities , l) Verification of implementation of Corrective actions for the minor non conformities by off site review, and m) Any other requirements prescribed by the Certification Body. The certification Body shall grant certification after ensuring complete compliance to the Certification Criteria and certification scheme requirements and all non conformances have been addressed in accordance with Clause 4.3.1 above. There shall be no conditional grant of certification. On grant of certification, the Certification body shall inform the organization and issue a Certificate, uniquely identified, to the organization indicating the names of the product(s) certified, the certification criteria against which the certification has been awarded, effective date, validity date, and the name and address of the organization site where certified as a minimum.. No Brand names of the Ayush Products shall be mentioned on the Certificate document or any other document intimating grant of certification. Licensed formulation as given on the licences shall be mentioned on the certificate document or any other document intimating grant of certification.. SectionIVCertificationProcessVersion1 Page7of13

4.3.5 4.3.6 4.3.7

4.4 4.4.1

4.4.2

4.4.3

4.4.4

4.4.5

4.4.6

The effective date of certification shall not be before the date of decision to grant the product certification to the organization. The certificate for product certification shall be for a maximum period of 3 years from the date of decision to grant the product certification. The certification decision shall clearly inform the manufacturing organization that they have to seek approval from QCI (representing the Department Ayush) for using the Ayush Certification Mark on their products. Surveillance Evaluation Surveillance evaluations of the certified sites during the first certification cycle shall be carried out at a frequency of at least once in six months, ensuring that the gap between two surveillance evaluations does not exceed six months. The Certification Body may allow a grace period of one month based on valid grounds beyond which delays shall lead to suspension of the certificate. The certification body shall ensure that critical steps in an operation or a combination of production operations on a given days are witnessed , their controls verified , and samples drawn for testing both in the factory and for independent testing during the surveillance evaluation. Planning for surveillance evaluations shall ensure this In case where the unit is certified to a number of products of different dosage forms under the same certificate, certification body shall plan for surveillance evaluation with a view to covering all dosage forms, and as many Ayush products within each dosage form during the certification cycle through independent testing of factory samples and market samples..The certification body shall draw more samples of products registering higher volumes in production For each dosage form certified, the certification body shall ensure that as a minimum at least one sample of each dosage form from the factory and two from the market are drawn per annum for independent testing . During the surveillance evaluation, the evaluators shall as a minimum check and report on the following; a) Compliance to the requirements of the certification criteria. b) Status of hygienic conditions c) Compliance to the Internal quality assurance protocol d) Handling and disposal of non conforming products e) Actions taken on discrepancies observed during the previous evaluation, failure of samples if any reported and informed to the manufacturing unit; f) Draw samples for factory testing and testing in independent laboratory g) The continued availability of the manufacturing machinery and test equipment and changes since the previous evaluation. In the event of changes the evaluator shall ascertain if they are adequate for control of processes and testing of the products. h) Information on production of Ayush products and the names of consignees to whom Ayush marked products have been despatched for the purpose of market sampling. If any non conformities are observed, the same shall be categorized as either a Major or a Minor. The non conformity report shall be provided to the client in writing, generally on site, for correction and corrective action. Details of the same shall be reported in the Surveillance evaluation report. SectionIVCertificationProcessVersion1 Page8of13

4.4.7

The certification body after completion of the first certification cycle may increase or decrease the frequency of surveillance evaluation based on the performance of the manufacturing unit not less than once a year in any case. 4.4.8 The frequency of surveillance evaluation maybe reduced to once in a year provided there have been no Major non conformities, failure of samples or complaints during the previous three years. The certification body shall revert to the normal frequency immediately in case any change in this situation occurs. 4.4.9 If the surveillance evaluation results in an infructuous visit due to any reason, and neither the production is witnessed nor products drawn for testing either in the factory or for independent testing, the CB shall conduct another surveillance evaluation. Such additional evaluations may be charged to the certified unit as decided by the Certification Body. 4.5 Market samples 4.5.1 Samples of certified products shall be purchased from the market or procured from organized consumers and tested in NABL accredited laboratories for ascertaining compliance to requirements of the Certification Criteria. 4.5.2 The certification body shall draw a minimum of 2 samples from each dosage form product group certified from the market for each client in a year. 4.5.3 In case where the unit is certified to a number of products of different dosage forms under the same certificate, certification body shall attempt to draw the market samples in a manner so that all dosage forms and practically the entire range of products within each dosage form are covered in factory and market sampling within a certification cycle. 4.5.4 Market samples shall be drawn in the original packaging and product integrity shall be ensured by the certification body. 4.6 Failure of sample of certified product, drawn from the factory or the market, to comply to criteria requirements shall be communicated to the certified manufacturing unit for investigation, root cause analysis and proposed corrective actions within 15 days of intimation. The CB shall respond to the proposed corrective actions within 5 days and the manufacturer shall implement the corrective actions within one month from acceptance of the corrective actions by the CB. 4.7 Depending on the nature of the failure reported, the CB shall decide on one or any of the following ; a) Draw additional samples of the product manufactured around the same time from the market; b) Organize for an additional surveillance evaluation immediately c) Ensure fresh sample is tested in the factory; d) Increase the frequency of surveillance evaluation e) Increase the number of market samples The manufacturer shall be informed of the decision taken. 4.8 When the failure of the sample is in requirements relating to Contaminants the CB shall advise the manufacturer to; a) Stop despatches of the failing Batch if stocks are available either at the site or in their warehouses; b) Recall the failing Batch from the market;

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Identify all Ayush products manufactured with same starting herbal material, or those manufactured during the same time under similar controls, and examine their Batch processing records and Batch packaging records and retest the Reference samples of these Batches in the custody of the Manufacturer; or Suspend the certification, till adequate and effective corrective actions are d) taken. 4.9 Suspension 4.9.1 The certification body shall issue instructions to the certified manufacturing units for suspension of certification when; a) any sample fails to conform to the requirements relating to Contaminants b) 2 consecutive samples, from the factory or market, as determined by date of manufacture, fail to conform to the requirements of the product requirements other than contaminants; c) Unsatisfactory performance during two consecutive Surveillance evaluations on account of any of these aspects is observed; i. Failure of sample on factory testing (in case of failure of contaminants 4.9.1 a) above applies) ii. Unsatisfactory hygienic conditions iii. Important testing equipment not calibrated iv. Testing equipment out of order and no alternate arrangements for testing v. Non implementation of Internal Quality Assurance Protocol vi. Non availability of testing personnel and absence of alternate arrangements c) Unsatisfactory hygienic conditions of serious nature during a surveillance evaluation. 4.9.2 The certification body shall issue due notice of at least one week for suspension of certification to the manufacturing unit. In case of serious failures mentioned at 4.9.1 a) and c) above , the notice may not be required. 4.9.3 On receipt of instructions for suspension of certification, the certified units shall suspend using Ayush certification mark on Ayush products being manufactured by them with immediate effect. The manufacturing unit shall be advised to undertake a root cause analysis and identify the necessary corrective actions for resolving the same. 4.9.4 While under suspension, the certification body shall ensure that despatches of certified Ayush products to the market/customer are withheld until the product in stock has been reassessed for conformity to the criteria. The manufacturing organization shall reassess the quality of the products in stock and the CB shall verify this reassessed stock for conformity to the certification criteria before allowing its despatch. 4.9.5 The certification body shall revoke suspension only when ; a) Corrective actions have been taken and verified by the certification body. b) Reports of Samples of Ayush products manufactured after corrective actions, both during factory and independent testing confirm compliance to Criteria requirements.

c)

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4.9.6

Suspension shall not exceed a period of six months. The manufacturing units inability to resolve issues relating to suspension within this period shall lead to cancellation of certification. 4.10 Renewal 4.10.1 The certification body shall send the Renewal notice to the certified units at least four months prior to expiry of certificate validity period. 4.10.2 The manufacturing organization shall apply for renewal in the prescribed format along with fee, if any prescribed by the CB at least 3 months before expiry of the certification. 4.10.3 The certification body shall review the performance of the certified unit who has sought renewal of the Certificate, with respect to compliance to certification criteria during the entire certification cycle, prior to a decision on the renewal of the certificate. 4.10.4 The review shall be based on a) surveillance and renewal evaluation reports, b) Quantum of Ayush products conforming to criteria expressed as percentage of quantity manufactured c) Handling and disposition of non conforming products d) Test reports for samples drawn from the factory and the market, e) Any suspension of certificate during the previous validity period; f) corrective actions taken g) complaints if any received, h) Adverse information, if any. 4.10.5 Renewal of certificate shall be based on the satisfactory performance of the certified units. 4.10.6 The certification Body shall not renew certification with conditions for compliance to be verified subsequently. There shall be no conditional renewal of certification. 4.10.7 When performance of the certified units is not satisfactory, the certification body shall withhold the renewal of the certificate to the manufacturing organization clearly stating the reasons and give time for effecting corrective actions. The verification and decision on renewal should be taken within 3 months of the expiry date. 4.10.8 The corrective actions shall be verified generally on site unless the CB can verify the same off site prior to considering for renewal of certificate. The justification for off site review shall be recorded. 4.10.9 The renewal shall be effected from the date of the expiry of the previous certificate and the intervening period shall be treated as period of suspension and clearly stated on the Certificate. The manufacturing unit shall not claim certification or use the Certification Mark during this period. 4.10.10 In case the manufacturing unit does not complete satisfactorily actions within three months, the certificate shall stand expired from the date of expiry of previous validity. 4.10.11 When a certificate is not renewed, it shall expire at the end of validity period. 4.11 Cancellation 4.11.1 Certification body shall cancel the certificate when ; a) Certified unit contravenes the terms and conditions of certification and provisions of Ayush certification scheme like repeated failures of samples, suspension of SectionIVCertificationProcessVersion1 Page11of13

4.11.2

4.12 4.12.1 4.12.2 4.12.3 4.12.4

4.12.5 4.12.6

4.12.7

4.13 4.13.1

4.13.2

certificate, inadequate corrective actions, lack of compliance to Internal quality protocol, misuse of Ayush Certification Mark(s) etc b) Ayush products are failing and not conforming to the requirements of the Certification Criteria and the corrective actions taken are not ensuring compliance, or the proposed plan for corrective actions will take a considerable time beyond 6 months for implementation; Certification body shall cancel the product certification certificate at the request of the certified unit, if the operation(s) in the certified units premises can no longer be carried due to reasons of natural calamities such as flood, fire, earthquake etc, lock out declared by the management, or closure of business operations etc. Change of location/Ownership/Name The certified organization shall inform the CB of any change in the location of the manufacturing unit. On receipt of such information, the certification body shall issue instructions to the certified manufacturing units for suspension of certification with immediate effect. The manufacturing unit shall be subject to an evaluation at the new site like an Initial Evaluation of an applicant. If the evaluation is satisfactory, the CB shall transfer the Certificate to the new location and the manufacturing unit shall be permitted to affix the Certification mark to the Ayush products produced therein. The CB shall endorse the change of premises on the Certificate. In the event of change of Ownership, the organization shall provide necessary documentary evidence. The new management of the organization shall submit its acceptance to the agreement for Certification with the CB, Internal Quality Assurance Protocol and payment of fees. The same process shall be followed as and when an existing applicant undergoes a change in management. Such changes shall not call for a visit to the production site. In case of change of Name, the manufacturer shall inform the change in the name to the CB supported with documentary evidence, and if satisfied the CB shall endorse the Certificate in the new name. Extension of scope Extension of scope of certificate for inclusion of additional dosage forms and products therein under the same certificate shall be done after: a) ascertaining that the certified organization has requisite resources required e.g. raw materials, process controls, manufacturing machinery, test facilities and technical skills .for dosage forms and products under extension of scope, through an on site evaluation, and b) test reports for sample of products of the new dosage form are on independent testing found conforming to requirements of the Criteria For extension of scope of certificate for inclusion of additional products within an existing dosage form of the Ayush Product under the same certificate, the certification body shall a) draw samples of additional products as per sampling plan at Cl 4.2.9 for independent testing. b) Process for extension of scope for the additional products on the basis of test reports of additional products in the same dosage form, provided by the SectionIVCertificationProcessVersion1 Page12of13

4.13.3

4.14 4.14.1 a) b) c) d) e) f) g) h) i) 4.14.2 4.14.3 4.15 4.15.1

4.15.2 4.15.3

manufacturer, subject to conformity of samples on independent testing mentioned at a) above. The extension of scope shall be clearly mentioned in the certificate document along with its date of inclusion for avoiding any misrepresentation or misinterpretation. Irrespective of the date of inclusion, the validity of the Certificate shall remain unchanged. Certificate The CB shall provide a certification document to the certified client that clearly conveys, or permits identification of: the name and geographic location of the client whose products have been certified the dates of granting, extending or renewing certification; the expiry date or recertification due date consistent with the recertification cycle; a unique identification code; the certification criteria, including issue number and/or revision, against which the product(s) are certified; the scope of certification with respect to product (s) as applicable at the identified site; the name, address and certification mark of the certification body; other marks (e.g. accreditation symbol) may be used provided they are not misleading or ambiguous; any other information required by the certification criteria used for certification; in the event of issuing any revised certification documents, a means to distinguish the revised documents from any prior obsolete documents The effective date on a certification document shall not be before the date of the certification / recertification decision. The formal certification documentation shall include the signature of the individual(s) of the certification body assigned such responsibility. Fee A fee to be charged to the organization for various activities of the Ayush Product certification scheme, without any discrimination between units, geographical location, size of the unit. The CBs fee structure shall be publically accessible and also be provided on request. CB shall notify and obtain consent to its fee structure from the organizations prior to grant of certification. As and when the fee undergoes a change, the same shall be communicated to all including applicants and the manufacturing units certified under this scheme of certification for their acceptance.

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